Wilson's disease with extensive white and gray matter MRI abnormalities: a case report
Sudan Medical Monitor. 2008; 3 (2): 61-64
em Inglês
| IMEMR
| ID: emr-103626
ABSTRACT
Wilson disease is an autosomal recessive disease, characterized by excessive accumulation of copper in the body, particularly in the liver, brain, cornea and kidney, with variable clinical manifestations. The outcome of treatment depends on early diagnosis of the disease before major irreversible tissue destruction occurs. Early diagnosis might be difficult because of its diverse clinical manifestations. We herein report on a patient with severe clinical and imaging manifestations. The patient showed cerebral atrophy and extensive abnormalities in frontal lobes, the putamen, the thalami, cerebral peduncles and posterior aspects of the occipital lobes. Such wide spread changes involving the white matter as well as the gray matter is rarely reported
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Índice:
IMEMR (Mediterrâneo Oriental)
Assunto principal:
Putamen
/
Atrofia
/
Tálamo
/
Encéfalo
/
Tegmento Mesencefálico
/
Imageamento por Ressonância Magnética
/
Lobo Frontal
/
Degeneração Hepatolenticular
/
Lobo Occipital
Tipo de estudo:
Relato de Casos
/
Estudo de rastreamento
Limite:
Feminino
/
Humanos
Idioma:
Inglês
Revista:
Sudan Med. Monit.
Ano de publicação:
2008
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